Visualising Clinical and Genetic Data

2. The method of claim 1, further comprising determining a weight value for each path from a first observed phenotype over a first disorder to a first genetic property based on a number of observed phenotypes that are associated with the first disorder in the path and determining the association value based on the weight value.

3. The method of claim 1, wherein detecting the user interaction comprises detecting user interaction in relation to one of the multiple genetic properties indicative of a user selecting the one of the multiple genetic properties, and wherein re-arranging the arrangement of the association values comprises sorting the multiple observed phenotypes by the association value for the selected genetic property.

4. The method of claim 1, wherein detecting the user interaction comprises detecting user interaction in relation to one of the multiple observed phenotypes indicative of a user selecting the one of the multiple observed phenotypes, and wherein re-arranging the arrangement of the association values comprises removing genetic properties that have no paths to one or more remaining observed phenotypes after removal of the observed phenotype selected by the user.

5. The method of claim 1, wherein the arrangement of the association values is a matrix of at least one of the multiple observed phenotypes across genetic properties and a visual appearance of each field of the matrix is based on the association value associated with that field.

6. The method of claim 5, wherein the visual appearance comprises one of multiple predefined shadings indicative of a range of the association value.

9. The method of claim 7, further comprising determining a weight value for each path from a first observed phenotype over a first disorder and a first gene location to a first gene function based on the number of paths from the first observed phenotype to the first gene location and determining the association value based on the weight value.

10. The method of claim 9, further comprising normalising the weight value across the multiple gene locations.

11. The method of claim 1, further comprising filtering at least one the multiple observed phenotypes by physiological system.

12. The method of claim 1, further comprising displaying an indication of variants in whole genome sequencing data of the patient based on the association values for respective gene locations.

13. The method of claim 1, wherein accessing the first database or accessing the second database or both comprises accessing a graph database.